U.S. patent application number 10/729748 was filed with the patent office on 2004-06-17 for surface-treated plastic article and method of surface treatment.
Invention is credited to Shimoyama, Naoki, Uemura, Tadahiro, Yokota, Mitsuru.
Application Number | 20040114105 10/729748 |
Document ID | / |
Family ID | 18644647 |
Filed Date | 2004-06-17 |
United States Patent
Application |
20040114105 |
Kind Code |
A1 |
Shimoyama, Naoki ; et
al. |
June 17, 2004 |
Surface-treated plastic article and method of surface treatment
Abstract
The present invention relates to a surface-treated plastic
article including a thin layer composed of a polymer complex on the
surface. The surface-treated plastic article can be produced by a
treatment with at least one kind of aqueous solutions of polymers
having a weight average molecular weight of 200 or more. According
to the present invention, the plastic articles, such as contact
lenses, having superior transparency, wettability, oxygen
permeability, and mechanical properties can be provided.
Inventors: |
Shimoyama, Naoki; (Shiga,
JP) ; Yokota, Mitsuru; (Shiga, JP) ; Uemura,
Tadahiro; (Kanagawa, JP) |
Correspondence
Address: |
PHILIP S. JOHNSON
JOHNSON & JOHNSON
ONE JOHNSON & JOHNSON PLAZA
NEW BRUNSWICK
NJ
08933-7003
US
|
Family ID: |
18644647 |
Appl. No.: |
10/729748 |
Filed: |
December 5, 2003 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10729748 |
Dec 5, 2003 |
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|
09842402 |
Apr 26, 2001 |
|
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6689480 |
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Current U.S.
Class: |
351/159.78 |
Current CPC
Class: |
C08J 7/048 20200101;
C08J 7/056 20200101; G02B 1/043 20130101; C08J 2300/14 20130101;
Y10T 428/31667 20150401; Y10T 428/31928 20150401; Y10T 428/31935
20150401; A61M 1/16 20130101 |
Class at
Publication: |
351/177 |
International
Class: |
G02C 007/02 |
Foreign Application Data
Date |
Code |
Application Number |
May 10, 2000 |
JP |
136756/00 |
Claims
What is claimed is:
1. A method for surface treatment of a plastic article, comprising
a step of immersing said plastic article in an aqueous solution of
a polymer having a weight average molecular weight of 200 or
more.
2. A method for surface treatment of a plastic article according
claim 1, wherein said step further comprising: immersing in an
aqueous solution of a second polymer having a weight average
molecular weight of 200 or more.
3. A method for surface treatment of a plastic article according to
claim 1 or 2, wherein said plastic article is hydrogel.
4. A method for surface treatment of a plastic article according to
claim 3, wherein said plastic article has water content greater
than 15%.
5. A method for surface treatment of a plastic article according to
claim 3, wherein said hydrogel comprises at least one of a silicon
atom and a fluorine atom.
6. A method for surface treatment of a plastic article according to
claim 5, wherein said hydrogel has oxygen permeability coefficient
greater than 50.times.10.sup.-11 (cm.sup.2/sec)
[mlO.sub.2/(ml.multidot.hPa)].
7. A method for surface treatment of a plastic article according to
claim 1 or 2, wherein said plastic article is a macromolecule
substantially not containing water.
8. A method for surface treatment of a plastic article according to
one of claim 1 or 2, comprising a step of immersing said plastic
article in an aqueous solution having a pH of 6 or less.
9. A method for surface treatment of a plastic article according to
one of claim 1 or 2, wherein said polymer having the weight average
molecular weight of 200 or more is a carboxyl functional
polymer.
10. A method for surface treatment of a plastic article according
to claim 9, wherein said carboxyl functional polymer is a polymer
selected from the group consisting of polymethacrylic acid,
polyitaconic acid, and a copolymer of methacrylic acid, maleic
acid, itaconic acid, or maleic anhydride and a reactive vinyl
monomer, or a mixture thereof.
11. A method for surface treatment of a plastic article according
to one of claim 1 or 2, comprising a step of immersing said plastic
article in an aqueous solution having a pH of 8 or higher.
12. A method for surface treatment of a plastic article according
to claim 1 or 2, wherein said polymer having the weight average
molecular weight of 200 or more is a polyethyleneimine.
13. A method for surface treatment of a plastic article according
to claim 2, wherein said second polymer having the weight average
molecular weight of 200 or more is a nonionic water-soluble
polymer.
14. A method for surface treatment of a plastic article according
to claim 13, wherein said nonionic water-soluble polymer is a
polymer selected from the group consisting of polyacrylamide,
polydimethylacrylamide, polyvinyl pyrrolidone, polyethylene glycol,
polyethylene oxide, and polyvinyl alcohol, or a mixture
thereof.
15. A surface-treated plastic article comprising a thin layer of a
polymer complex on the surface of said surface-treated plastic
article, wherein the polymer complex is formed with a polymer
having a weight average molecular weight of 200 or more and a base
material.
16. A surface-treated plastic article according to claim 15,
wherein the thin layer further comprises a second polymer complex
formed with the second polymer having a weight average molecular
weight of 200 or more and said first polymer having the weight
average molecular weight of 200 or more.
17. A surface-treated plastic article according to claim 15 or 16,
wherein said plastic article is hydrogel.
18. A surface-treated plastic article according to claim 17,
wherein said hydrogel comprises at least one of a silicon atom and
a fluorine atom.
19. A surface-treated plastic article according to claim 18,
wherein said hydrogel has water content greater than 15%.
20. A surface-treated plastic article according to claim 19,
wherein said hydrogel has oxygen permeability coefficient greater
than
50.times.10.sup.-11(cm.sup.2/sec)[mlO.sub.2/(ml.multidot.hPa)].
21. A surface-treated plastic article according to claim 15 or 16,
wherein at least one of said polymers having the weight average
molecular weight of 200 or more is a carboxyl functional
polymer.
22. A surface-treated plastic article according to claim 21,
wherein said carboxyl functional polymer is a polymer selected from
the group consisting of polymethacrylic acid, polyitaconic acid,
and a copolymer of methacrylic acid, maleic acid, itaconic acid or
maleic anhydride and a reactive vinyl monomer, or a mixture
thereof.
23. A surface-treated plastic article according to claim 15 or 16,
wherein said surface- treated plastic article exhibits absorptions
at 1720 cm.sup.-1 band, 1404 cm.sup.-1 to 1442 cm.sup.-1 band, and
1556 cm.sup.-1 band in the infrared absorption spectrum based on an
attenuated total reflection spectroscopy.
24. A surface-treated plastic article according to claim 16,
wherein said second polymer having the weight average molecular
weight of 200 or more is a nonionic water-soluble polymer.
25. A surface-treated plastic article according to claim 24,
wherein said nonionic water-soluble polymer is a polymer selected
from the group consisting of polyacrylamide,
polydimethylacrylamide, polyvinyl pyrrolidone, polyethylene glycol,
polyethylene oxide, and polyvinyl alcohol, or a mixture
thereof.
26. A surface-treated plastic article according to claim 19,
wherein said polymer having the weight average molecular weight of
200 or more is polymethacrylic acid, and said surface-treated
plastic article is a contact lens containing at least one of a
silicon atom and a fluorine atom.
27. A surface-treated plastic article according to claim 26,
wherein said contact lens has oxygen permeability coefficient
greater than 50.times.10.sup.-11
(cm.sup.2/sec)[mlO.sub.2/(ml.multidot.hPa)].
Description
BACKGROUND OF THE INVENTION
[0001] 1. Field of the Invention
[0002] The present invention relates to a method for surface
treatment of a plastic article and a surface-treated plastic
article. In particular, the present invention relates to a
surface-treated plastic article exhibiting superior hydrophilicity,
that is, wettability, and superior deposition resistance, that is,
lipid-fouling resistance, etc., which has been surface-treated
without degradation of properties as the plastic article.
Specifically, the surface-treated plastic article according to the
present invention is appropriately used for contact lenses and
intraocular lenses, or medical devices, such as catheters and
artificial kidneys.
[0003] 2. Description of the Related Art
[0004] In recent years, plastic articles have been proposed for
many purposes. Among those, various plastic articles containing
silicon or fluorine have been proposed for contact lenses because
of the excellent oxygen permeability.
[0005] The plastic articles containing silicon or fluorine are,
however, insufficient in wettability, and an improvement in the
wettability has been demanded. In particular, various methods have
been proposed in order to improve the lens performance (fitting
characteristics, comfort etc.) in eyes by surface modification of
contact lenses. For example, in US Pat. No. 4,214,014, a method, in
which the wettability is imparted to a contact lens by a plasma
treatment in an oxygen atmosphere, is disclosed. In JP-A-8-227001,
a method, in which the wettability is imparted to a silicone
containing hydrogel contact lens by a plasma treatment in the
atmosphere of oxygen and/or carbon dioxide gas, is disclosed.
[0006] The aforementioned conventional techniques improved the
wettability, however, there have been problems in that the material
quality of the plastic article was degraded due to the oxygen gas.
In addition to this, there was a significant problem in that the
wettability varied with time due to washings and a long term of use
so as to become hydrophobic.
SUMMARY OF THE INVENTION
[0007] The inventors of the present invention earnestly researched
in order to solve the aforementioned problems, and discovered a
method for surface treatment of the plastic article, to get good
and stable wettability of the surface without variation with time
keeping the goodinherent properties of the plastics unchanged, so
that the present invention was made. Accordingly, it is an object
of the present invention to provide a surface-treated plastic
article having high transparency and high oxygen permeability,
exhibiting excellent wettability and superior mechanical
properties, and appropriately used for, in particular, contact
lenses and medical devices such as catheters. It is another object
of the present invention to provide a method for surface treatment
of the aforementioned plastic article.
[0008] The present invention resides in the following features in
order to achieve the aforementioned objects. According to a first
aspect of the present invention, a method for surface treatment of
a plastic article, in which the plastic article is treated with at
least one kind of aqueous solutions of polymers having a weight
average molecular weight of 200 or more, is provided. According to
a second aspect of the present invention, a plastic article,
surface-treated with the polymer having a weight average molecular
weight of 200 or more, is provided. According to a third aspect of
the present invention, a surface-treated plastic article, including
a thin layer composed of a polymer complex on the surface, is
provided.
BRIEF DESCRIPTION OF THE DRAWING
[0009] FIG. 1 is a diagram showing ATR spectra of plastic articles
treated with PAA and not treated, and a differential spectrum
therebetween.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0010] As the surface-treated plastic article according to the
present invention, plastic articles primarily composed of
homopolymers of various monomers described below, copolymers of
these monomers and other monomers, polymers containing silicon in
at least one of the main chain and the side chain thereof, for
example, polymers containing a siloxane bond or an organic silane
group, e.g., trimethylsilyl group, or polymers containing a
carbon-fluorine bond can be mentioned.
[0011] As specific examples of the monomers for producing the
aforementioned polymers, methacrylic acid (hydroxy)alkyl esters,
for example, methyl methacrylate and 2-hydoxyethyl methacrylate,
methacrylic esters containing silicon, for example,
tris(trimethylsiloxy)silylpropyl methacrylate, methacrylic esters
containing fluorine, and polydimethylsiloxane having a double-bond
at a single terminal or at each of both terminals, can be
mentioned.
[0012] As the monomer which can copolymerize, mono-functional
monomers, for example, methacrylic acid ester-based monomers,
aromatic vinyl monomers, and heterocyclic vinyl monomers,
multi-functional monomers, for example, di-functional
methacrylates, tri-functional methacrylates, tetra-functional
methacrylates, aromatic divinyl monomers, and aromatic diaryl
monomers, etc., can be mentioned.
[0013] As specific examples of the mono-functional monomer, alkyl
methacrylates, for example, methyl methacrylate and ethyl
methacrylate, carboxylic acids, for example, methacrylic acid,
cycloalkyl methacrylates, for example, cyclohexyl methacrylate,
halogenated alkyl methacrylates, for example, trifluoroethyl
methacrylate and hexafluoroisopropyl methacrylate, hydroxyalkyl
methacrylates having a hydroxyl group, for example, 2-hydroxyethyl
methacrylate and 2,3-dihydroxypropyl methacrylate, acrylamides, for
example, acrylamide, N,N-dimethylacrylamide, and
N,N-diethylacrylamide, methacrylic acid esters having a siloxanyl
group, for example, tris(trimethylsiloxy)silylp- ropyl methacrylate
and bis(trimethylsiloxy)methylsilylpropyl methacrylate, aromatic
vinyl monomers, for example, styrene and vinylpyridine, styrene
derivatives having a siloxanyl group, for example,
tris(trimethylsiloxy)silylstyrene, styrene derivatives having
fluorine, for example, pentafluorostyrene, and heterocyclic vinyl
monomers, for example, N-vinyl pyrrolidone, can be mentioned.
[0014] As specific examples of the di-functional monomer, ethylene
glycol dimethacrylate, diethylene glycol dimethacrylate, bisphenol
A dimethacrylate, bisphenol A dimethacrylate ethylene oxide adduct
or urethane-modified substances thereof, propylene glycol
dimethacrylate, glycerol dimethacrylate, neopentyl glycol
dimethacrylate, etc., can be mentioned. As specific examples of the
tri-functional monomer, trimethylolpropane trimethacrylate,
trimethylolpropane trimethacrylate ethylene oxide adducts, etc.,
can be mentioned. As specific examples of the tetra-functional
monomer, tetramethylolmethane tetramethacrylates, etc., can be
mentioned. As specific examples of the aromatic divinyl monomers,
divinylbenzene, etc., can be mentioned. As specific examples of the
aromatic diaryl monomers, diaryl phthalate, etc., can be mentioned.
As specific examples of other multi-functional monomers,
bismaleimide, aryl methacrylate, etc., can be mentioned.
[0015] The plastic article used in the present invention may be
water containing hydrogel, may be a rubber-like polymer (elastomer)
not containing water, or may be a hard polymer containing no water
or containing small amounts of water depending on the rates of
these monomers in copolymerization and the kinds of used
monomers.
[0016] The surface-treated plastic article according to the present
invention may be transparent or may be opaque, although since the
hydrogel and the plastic article containing at least one of a
silicon atom and a fluorine atom are superior in oxygen
permeability, those are preferably used for the optical articles,
so that the transparency is preferably imparted thereto.
[0017] Regarding the polymer constituting the surface-treated
plastic article according to the present invention, in the case in
which the polymer is hydrogel, the combination of a hydrophilic
monomer and a cross-linking agent and the combination of a
hydrophobic monomer, a hydrophilic monomer, and a cross-linking
agent are preferably used. For example, the combination of
2-hydoxyethyl methacrylate and ethylene glycol dimethacrylate, and
the combination of 2,3-dihydroxypropyl methacrylate, methyl
methacrylate, and diethylene glycol dimethacrylate are mentioned.
In the case in which the hydrogel contains at least one of a
silicon atom and a fluorine atom, the combinations of methacrylic
acid esters having siloxanyl group, for example,
tris(trimethylsiloxy)silylpro- pyl methacrylate or a silicone
component, for example, polydimethylsiloxane containing double
bonds at both ends, a component containing fluorine, for example,
hexafluoroisopropyl methacrylate, a hydrophilic component, for
example, N,N-dimethylacrylamide and N-vinyl pyrrolidone, and a
cross-linking agent are mentioned. In the case of plastic articles
which contains substantially no water and contains the component
containing silicon and/or fluorine atom, the content of the
component containing the silicon atom or the fluorine atom, may be
100% by weight, although the content is preferably 5% by weight or
more, more preferably is 30% by weight or more, from the view point
of the maintenance of the balance between the oxygen permeability
and the mechanical properties.
[0018] Regarding the method for the polymerization, conventional
methods can be used. The surface-treated plastic article according
to the present invention may contain an ultraviolet absorbent, a
coloring matter, colorant, etc.
[0019] In the production of the plastic article used in the present
invention, in order to facilitate the polymerization, thermal
polymerization initiators or photopolymerization initiators,
typified by peroxides and azo compounds, are preferably blended. In
the thermal polymerization, the initiator exhibiting optimal
decomposition performance at the desired reaction temperature is
selected and used. In general, the peroxide-based initiators and
azo-based initiators, having a half-life of 10 hours at a
temperature of 40.degree. to 120.degree. C., are appropriate. As
the photopolymerization initiator, carbonyl compounds, peroxides,
azo compounds, sulfur compounds, halogen compounds, metallic salts,
etc., are mentioned. These polymerization initiators are used
solely or as mixtures, in an amount up to about 1% by weight.
[0020] In the production of the plastic article used in the present
invention, polymerization solvents can be used. As the solvent,
various organic and inorganic solvents can be applied. Although not
specifically limited, for example, water, various alcohol solvents,
e.g., methanol, ethanol, propanol, 2-propanol, butanol, and
tertbutanol, butanol, various aromatic hydrocarbon-based solvents,
e.g., benzene, toluene, and xylene, various aliphatic
hydrocarbon-based solvents, e.g., hexane, heptane, octane, decane,
petroleum ether, kerosene, ligroin, and paraffin, various
ketone-based solvents, e.g., acetone, methyl ethyl ketone, and
methyl isobutyl ketone, various ester-based solvents, e.g., ethyl
acetate, butyl acetate, methyl benzoate, and dioctyl phthalate, and
various glycol ether-based solvents, e.g., diethyl ether,
tetrahydrofuran, dioxane, ethylene glycol dialkyl ether, diethylene
glycol dialkyl ether, triethylene glycol dialkyl ether,
tetraethylene glycol dialkyl ether, and polyethylene glycol dialkyl
ether, can be mentioned. These can be used solely or as
mixtures.
[0021] The plastic article used in the present invention can be
produced by, for example, the following method.
[0022] That is, polymers may be molded into rods and plates at
first, and then, may be worked into desired shape. Other known
techniques, such as the mold polymerization and the spin cast
polymerization, may be used. Regarding the molding into fibers and
films, polymers may be molten or dissolved in solvents, and then,
may be spun or subjected to the extrusion molding. As an example,
the case in which the plastic article used in the present invention
is produced by the mold polymerization will be explained below. The
monomer mixture of the aforementioned monomer composition and the
polymerization initiator are put in the space between a pair of
molds having specified shapes, and are molded into the shape of the
molds by the photopolymerization or the thermal polymerization. The
molds are made of resins, glass, ceramics, metals, etc. In the
photopolymerization, optically transparent materials are used, and
usually, the resins and the glass are used. In the production of
the plastic articles, in many cases, a pair of faced molds form the
space, and a monomer mixture is put into the space, although a
gasket may be concurrently used for imparting specified thickness
to the plastic article and for preventing monomer mnixture liquid
put into the space from leaking. The molds, in which the monomer
mixtures are put into the spaces, may be subsequently subjected to
irradiation of an activation ray, such as an ultraviolet ray, or
may be subjected to heating and polymerization in an oven or a
liquid bath. A Double-polymerization method in which the thermal
polymerization is performed after the photopolymerization, or, on
the contrary, the photopolymerization is performed after the
thermal polymerization, may be concurrently used. Regarding the
photopolymerization, in general, the light, primarily including the
ultraviolet ray, using, for example, a mercury lamp and an insect
collection lamp as the light source, is irradiated for a short
time, usually within one hour. Regarding the thermal
polymerization, in order to maintain the optical uniformity and
quality of the plastic article, and to improve the reproducibility,
it is appropriate to gradually raise the temperature from the
vicinity of room temperature to 60.degree. to 200.degree. C. over a
period of time several hours to several tens of hours.
[0023] It was discovered that very simple treatment of immersing
the plastic articles in at least one kind of aqueous solutions
selected from the group consisting of high molecular weight acids,
high molecular weight bases, and water-soluble polymers, each
having the weight average molecular weight of 200 or more,
exhibited surprising effects of improving the hydrophilicities
(water wettabilities) of the plastic articles, and of maintaining
these, so that the present invention was made.
[0024] In particular, the high molecular weight acids and bases
having average molecular weights of 500 or more are preferably used
from the viewpoint of preventing the plastic articles from
degrading due to the acids and the bases. Furthermore, regarding
the treatment of the hydrogel plastic articles, the high molecular
weight acids and bases having average molecular weights of 1,000 or
more are preferably used.
[0025] Regarding the treatment with aqueous solutions of the
polymer having the weight average molecular weight of 500 or more,
since the polymers do not penetrate into the inside of the plastic
articles, the plastic articles are not likely to degrade due to the
cleavage of at least one of the main chains and side chains.
[0026] In order to effectively improve the hydrophilicity
(wettability) and to maintain the effects for a long term, the
polymer aqueous solution having a pH of 4 or less or a pH of 8 or
more is preferably used. The treatment with the polymer aqueous
solution, having a pH of more than 4 and less than 8, may take a
long time to produce the hydrophilicity, and in some cases,
sufficient hydrophilicity may not be produced.
[0027] The treatment temperature is usually 1.degree. to 99.degree.
C., and preferably in the vicinity of Tg of the base material to be
treated. The treatment time is usually 1 to 72 hours in order to
produce sufficient effect of treating. The present invention is
not, however, limited to these conditions.
[0028] Regarding the present invention, two kinds of polymer
aqueous solutions may be used. That is, immersion in the first
polymer aqueous solution, treatment, and washing are performed, and
thereafter, immersion in the second polymer aqueous solution, and
treatment are performed. Accompanying this, the natures of the
surface, such as ionicity and nonionicity, can be appropriately
changed.
[0029] As the acid, having a weight average molecular weight of 200
or more, used for the surface treatment of the plastic article, a
carboxyl functional polymer, a polymer having the --SO.sub.3H
group, etc., can be mentioned. AS the high molecular weight base, a
polymer having the --NH group, or the --NH.sub.2 group, etc., can
be mentioned.
[0030] In particular, in the present invention, when the plastic
article is hydrogel, a carboxyl functional polymer is preferably
used. The carboxyl functional polymer means a polymer having the
--COOH group in the molecule. Most of all, a polymer selected from
the group consisting of polymethacrylic acid, polyitaconic acid,
and copolymers of methacrylic acid, maleic acid, itaconic acid, or
maleic anhydride and a reactive vinyl monomer, or a mixture thereof
can be appropriately used.
[0031] The weight average molecular weight of these carboxyl
functional polymers are preferably 5,000 or more, and more
preferably are 20,000 or more since the wettability of the surface
can be improved without degradation of mechanical properties of the
hydrogel. By using the aforementioned high molecular weight,
carboxyl functional polymers, strong polymer complexes can be
formed with the hydrophilic polymers in the hydrogel base
materials, and the effects thereof can be maintained for further
long term.
[0032] As the carboxyl functional polymer, poly acrylic acid and
alternative copolymer of maleic anhydride with vinyl monomer can be
appropriately used from the viewpoint of the ability of forming
polymer complexes, the long term maintenance of the effects, and
the available ease of the high molecular weight products.
[0033] Regarding the treatment of the hydrogel plastic article with
two kinds of polymer aqueous solutions, in the case in which the
aqueous solution of the carboxyl functional polymer is used as the
first polymer aqueous solution, the non-ionic water-soluble polymer
is preferably used as the second polymer aqueous solution. The
non-ionic water-soluble polymer means a water-soluble polymer not
containing an ionic group, and polyacrylamide,
polydimethylacrylamide, polyvinyl pyrrolidone, polyethylene glycol,
polyethylene oxide, and polyvinyl alcohol, or a mixture thereof are
preferably used. These non-ionic polymers form thin layers of
polymer complexes with the carboxyl functional polymers on the thin
layers of polymer complexes formed by the immersion treatment in
the first aqueous solutions, so that the properties of the surfaces
can be changed.
[0034] As the preferred embodiments of the surface-treated plastic
article according to the present invention, lenses, fibers, films,
etc., can be mentioned. In particular, the surface-treated plastic
article is appropriately used for optical articles, for example,
contact lenses, intraocular lenses, and plastic lenses, from the
viewpoint of excellent optical properties, high oxygen
permeability, excellent wettability, and mechanical properties, and
is also appropriately used for medical devices, such as catheters
and artificial kidneys, because of the wettability of the surface
and the sliding ease accompanying the wettability.
[0035] In the case in which the optical articles according to the
present invention are used for optical articles contacting with
corneas, such as contact lenses, the optical articles are
preferably hydrogel, and the water contents are preferably 15% or
more. By this, the movement of the lenses, which is required of the
optical articles contacting with corneas, becomes smooth, so that
the lenses can be worn with further safety.
EXAMPLES
[0036] The present invention will be explained using the following
examples, although the present invention is not limited to these
examples. Herein, measurements and evaluations were performed in
accordance with the following methods.
[0037] 1. Water Content
[0038] The plastic article was subjected to a hydration treatment,
and thereafter, the water content (%) was determined based on the
following formula:
Water content (%)=(W-WO)/W.times.100
[0039] wherein W designates the weight (g) of the plastic article
after the hydration treatment, and WO indicates the weight (g) of
the plastic article in a dry state.
[0040] 2. Dynamic Contact Angle
[0041] By using a plastic article having a size of about 5 mm by 10
mm by 0.1 mm, advancing dynamic contact angles relative to the
boric acid buffer solution having a pH of 7.1 to 7.3 were measured.
The immersion velocity was 0.1 mm/sec, and the depth of the
immersion was 7 mm.
[0042] 3. Static Contact Angle of Water
[0043] After water is removed from the surface by blowing with
nitrogen gas, the static contact angles of water were measured with
a CA-D type contact angle meter, manufactured by Kyowa Kaimen
Kagaku K. K., using water treated with the reverse osmosis
membrane.
[0044] 4. Wettability
[0045] The plastic article was immersed in the boric acid buffer
solution having a pH of 7.1 to 7.3. Thereafter, the plastic article
was pulled up, and the appearance of the surface was visually
observed so as to evaluate in accordance the following
criteria:
[0046] .circleincircle.: the surface of the plastic article is
uniformly wetted;
[0047] : a half or more of the surface area of the plastic article
is uniformly wetted;
[0048] .DELTA.: a half or more of the surface area of the plastic
article is not uniformly wetted; and
[0049] x: the surface of the plastic article is hardly wetted.
[0050] 5. Mechanical Properties
[0051] The plastic article having a size of about 15 mm by 10 mm by
0.1 mm was used as a sample, and the modulus and the elongation at
break were measured using Tensilon RTM-100 manufactured by Toyo
Baldwin K. K. The tensile speed was 100 mm/min, and the chuck
interval was 5 mm.
[0052] 6. Oxygen Permeability
[0053] The plastic article having a diameter of 15 mm was used as a
sample, and the oxygen permeability coefficient was measured using
Seikaken-type film-oxygen permeameter manufactured by Rikaseiki
Kogyo K. K. in water at 35.degree. C. The thickness of the sample
was adjusted by stacking a plurality of sheets if necessary.
Example 1
[0054] 60 parts by weight of tris(trimethylsiloxy)silylpropyl
methacrylate (abbreviated as TRIS), 40 parts by weight of
N,N-dimethylacrylamide (abbreviated as DMAA), 1 part by weight of
triethylene glycol dimethacrylate (abbreviated as 3G), and 10 parts
by weight of diethylene glycol dimethyl ether (abbreviated as
Diglyme) were uniformly mixed. After 0.2 parts by weight of
"Darocur1173", manufactured by Ciba Specialty Chemicals, as a
polymerization initiator was added thereto, the resulting monomer
mixture was degassed in an argon atmosphere. The degassed monomer
mixture was injected between plastic molds and was sealed in a
glove box in an atmosphere of nitrogen. Then, the light irradiation
was performed using an insect collection lamp at an illumination of
1 mW/cm.sup.2 for 30 minutes so as to perform polymerization.
Subsequently, the molds including the resulting plastic were
immersed in diethylene glycol dimethyl ether at 40.degree. C. for
30 minutes, and in addition to this, were immersed at 60.degree. C.
for 60 minutes, and then, the resulting plastic article to be
treated was released from the molds. As the immersion solution,
isopropyl alcohol was substituted for diethylene glycol dimethyl
ether, and the remaining monomers were extracted by heating at
60.degree. C. for 16 hours. The resulting plastic article to be
treated was washed two times with isopropyl alcohol. Thereafter,
the washed plastic article was immersed in a solution composed of
50 parts by weight of isopropyl alcohol and 50 parts by weight of
purified water for 30 minutes and then, was immersed in a solution
composed of 25 parts by weight of isopropyl alcohol and 75 parts by
weight of purified water for 30 minutes, and furthermore, was
immersed in purified water and was left standing for 16 hours, so
that isopropyl alcohol was completely removed from the plastic
article to produce the plastic article to be treated. The resulting
plastic article to be treated was immersed in an aqueous solution,
having a pH of 2.3, containing 15% by weight of polyacrylic acid
having an average molecular weight of 25,000 at 40.degree. C. for 8
hours. Subsequently, the resulting plastic article was sufficiently
washed with purified water, was put in a vial containing a boric
acid buffer solution having a pH of 7.1 to 7.3, and was sealed. The
resulting vial was put in an autoclave, and was subjected to a
boiling treatment at 120.degree. C. for 30 minutes. After the vial
was left standing for cooling, the plastic article was taken out of
the vial, and was immersed in the boric acid buffer solution having
a pH of 7.1 to 7.3. A water content, a dynamic contact angle,
wettability, a modulus, an elongation at break, and an oxygen
permeability coefficient of the resulting plastic article were
measured. The results thereof are shown in Table 1.
Example 2
[0055] A surface-treated plastic article was produced in a manner
similar to that in Example 1, except that the aqueous solution
containing polyacrylic acid in Example 1 was changed to an aqueous
solution, having a pH of 2.0, containing 20% by weight of
polyacrylic acid having an average molecular weight of 5,000. A
water content, a dynamic contact angle, wettability, a modulus, and
an elongation at break of the resulting plastic article are shown
in Table 1.
Example 3
[0056] A surface-treated plastic article was produced in a manner
similar to that in Example 1, except that the aqueous solution
containing polyacrylic acid in Example 1 was changed to an aqueous
solution, having a pH of 3.1, containing 1.2% by weight of
polyacrylic acid having an average molecular weight of 250,000. A
water content, a dynamic contact angle, wettability, a modulus, and
an elongation at break of the resulting plastic article are shown
in Table 1.
Comparative Example 1
[0057] A plastic article was produced in a manner similar to that
in Example 1, except that the treatment with the aqueous solution
containing polyacrylic acid in Example 1 was omitted. A water
content, a dynamic contact angle, wettability, a modulus, an
elongation at break, and an oxygen permeability coefficient of the
resulting plastic article are shown in Table 1.
Example 4
[0058] A surface-treated plastic article was produced in a manner
similar to that in Example 1, except that
tris(trimethylsiloxy)silylpropyl methacrylate in Example 1 was
changed to 68.75% by weight of the following compound M1
(abbreviated as SiOEMMA), 20.83% by weight of
N,N-dimethylacrylamide (abbreviated as DMAA), and 10.42% by weight
of N,N-methoxyethylacrylamide (abbreviated as MEAA), and the
treatment condition with the aqueous solution containing
polyacrylic acid in Example 1 was changed to at 60.degree. C. for
24 hours. A water content, a dynamic contact angle, wettability, a
modulus, and an elongation at break of the resulting plastic
article are shown in Table 1. 1
Example 5
[0059] A surface-treated plastic article was produced in a manner
similar to that in Example 4, except that the aqueous solution
containing polyacrylic acid in Example 4 was changed to an aqueous
solution, having a pH of 11.78, containing 30% by weight of
polyethyleneimine having an average molecular weight of 600, and
the treatment condition in Example 4 was changed to at 23.degree.
C. for 72 hours. A water content, a dynamic contact angle, and
wettability of the resulting plastic article are shown in Table
1.
Comparative Example 2
[0060] A plastic article was produced in a manner similar to that
in Example 5, except that the treatment with the aqueous solution
containing polyethyleneimine in Example 5 was omitted. A water
content, a dynamic contact angle, wettability, a modulus, and an
elongation at break of the resulting plastic article are shown in
Table 1.
Example 6
[0061] A surface-treated plastic article was produced in a manner
similar to that in Example 1, except that
tris(trimethylsiloxy)silylpropyl methacrylate in Example 1 was
changed to 70% by weight of the following compound M2 (abbreviated
as SiMAA2), and 30% by weight of N,N-dimethylacrylamide
(abbreviated as DMAA). A water content, a dynamic contact angle,
wettability, a modulus, and an elongation at break of the resulting
plastic article are shown in Table 1. 2
Example 7
[0062] A surface-treated plastic article was produced in a manner
similar to that in Example 1, except that
tris(trimethylsiloxy)silylpropyl methacrylate in Example 1 was
changed to 70% by weight of the following compound M3 (abbreviated
as SiMAA3), and 30% by weight of N,N-dimethylacrylamide. A water
content, a dynamic contact angle, wettability, a modulus, and an
elongation at break of the resulting plastic article are shown in
Table 1. 3
Example 8
[0063] A surface-treated plastic article was produced in a manner
similar to that in Example 1, except that the monomers in Example 1
were changed to 21.33 parts by weight of
tris(trimethylsiloxy)silylpropyl methacrylate, 42.67 parts by
weight of the compound M1 (abbreviated as SiOMMA), and 36 parts by
weight of N,N-dimethylacrylamide (abbreviated as DMAA), and the
aqueous solution in Example 1 was changed to an aqueous solution,
having a pH of 2.6, containing 5% by weight of polyacrylic acid
having an average molecular weight of 150,000. A water content, a
dynamic contact angle, wettability, a modulus, an elongation at
break, and an oxygen permeability coefficient of the resulting
plastic article are shown in Table 1.
[0064] A Fourier transform infrared spectrum of the surface-treated
plastic article according to the present invention measured by
Attenuated Total Reflection Spectroscopy (FTIR-ATR method) is shown
in FIG. 1. The result of the measurement by the FTIR-ATR method
regarding the plastic article according to Comparative Example 3,
and the differential spectrum, which is obtained by subtracting the
measurement result regarding Comparative Example 3 from the
measurement result regarding Example 8, are also shown in FIG. 1.
As is clear from FIG. 1, regarding the plastic article treated with
polyacrylic acid, designated by NS07 (PAA), carboxylic acid
(hydroxyl group) is increased as shown by an increase in 3,000 to
3,500 cm.sup.-1 band and an increase in 1,720 cm.sup.-1 band,
carboxylate is increased as shown by an increase in 1,404 to 1,442
cm.sup.-1 band and in 1,556 cm.sup.-1 band, and amide is decreased
as shown by a decrease in 1,645 cm.sup.-1 band compared to the
plastic article not treated with polyacrylic acid, designated by
NS07 (not treated). The increases of carboxylic acid and
carboxylate indicate that polyacrylic acid presents on the surface
of the surface-treated plastic article due to some interactions. On
the other hand, amide is believed to be derived from
dimethylacrylamide which is a hydrophilic component. Since this
amide bond is very stable, the amide bond is not normally
hydrolyzed by the aqueous solution having a pH of 2.6 or so.
Therefore, it is believed that polydimethylacrylamide in the base
material for the plastic article and polyacrylic acid formed a
polymer complex, a thin layer of the resulting complex was formed
on the surface, and as a consequence, the apparent density of the
amide bond of dimethylacrylamide was decreased so as to exhibit the
aforementioned differential spectrum.
Comparative Example3
[0065] A plastic article was produced in a mariner similar to that
in Example 8, except that the treatment with the aqueous solution
containing polyacrylic acid in Example 8 was omitted. A water
content, a dynamic contact angle, wettability, a modulus, an
elongation at break, and an oxygen permeability coefficient of the
resulting plastic article are shown in Table 1.
Example 9
[0066] A surface-treated plastic article was produced in a manner
similar to that in Example 8, except that the monomers in Example 8
were changed to 31.5 parts by weight of
tris(trimethylsiloxy)silylpropyl methacrylate (abbreviated as
TRIS), 31.5 parts by weight of the compound M2 (abbreviated as
SiMAA2), and 37 parts by weight of N,N-dimethylacrylamide
(abbreviated as DMAA). A water content, a dynamic contact angle,
wettability, a modulus, an elongation at break, and an oxygen
permeability coefficient of the resulting plastic article are shown
in Table 2.
Comparative Example 4
[0067] A plastic article was produced in a manner similar to that
in Example 9, except that the treatment with the aqueous solution
containing polyacrylic acid in Example 9 was omitted. A water
content, a dynamic contact angle, wettability, a modulus, an
elongation at break, and an oxygen permeability coefficient of the
resulting plastic article are shown in Table 2.
Example 10
[0068] A surface-treated plastic article was produced in a manner
similar to that in Example 1, except that the monomers in Example 1
were changed to 30 parts by weight of
tris(trimethylsiloxy)silylpropyl methacrylate (abbreviated as
TRIS), 30 parts by weight of tris(trimethylsiloxy)silylpr- opyl
acrylate (abbreviated as TRIS-A), and 40 parts by weight of
N,N-dimethylacrylamide (abbreviated as DMAA). A water content, a
dynamic contact angle, wettability, a modulus, and an elongation at
break of the resulting plastic article are shown in Table 2.
Example 11
[0069] 30.5 parts by weight of the compound M2 (abbreviated as
SiMAA2), 30.5 parts by weight of tris(trimethylsiloxy)silylpropyl
methacrylate (abbreviated as TRIS), 39 parts by weight of
N,N-dimethylacrylamide (abbreviated as DMAA), 1 part by weight of
triethylene glycol dimethacrylate (abbreviated as 3G), and 10 parts
by weight of diethylene glycol dimethyl ether (abbreviated as
Diglyme) were uniformly mixed. After 0.2 parts by weight of
"Darocur1173" manufactured by Ciba Specialty Chemicals, as a
polymerization initiator, was added thereto, a plastic article to
be treated was produced in a manner similar to that in Example 1.
On the other hand, 0.5 g of isobutylene-maleic anhydride copolymer
having a molecular weight of 160,000to 170,000 ("Isoban" 10,
manufactured by KURARAY CO., LTD.) was dispersed in 50 ml of 0.65N
NaOH solution, and the resulting solution was agitated at
90.degree. C. until the solution become transparent. Thereafter, 3
ml of 1N HCl was added, so that the pH was adjusted to 2.82.
[0070] In this polymer aqueous solution, the aforementioned plastic
article to be treated was immersed at 40.degree. C. for 5 hours.
Subsequently, the resulting plastic article was sufficiently washed
with purified water, was put in a vial containing a boric acid
buffer solution having a pH of 7.1 to 7.3, and was sealed. The
resulting vial was put in an autoclave, and was subjected to a
boiling treatment at 120.degree. C. for 30 minutes. After the vial
was left standing for cooling, the plastic article was taken out of
the vial, and was immersed in the boric acid buffer solution having
a pH of 7.1 to 7.3. A water content, a dynamic contact angle,
wettability, and an oxygen permeability coefficient of the
resulting plastic article were measured. The results thereof are
shown in Table 2.
Example 12
[0071] Methyl vinyl ether-maleic anhydride copolymer having a
molecular weight of 216,000 ("Gantrez" AN-119, manufactured by
International Specialty Products Inc.) was dispersed in purified
water, and the resulting solution was agitated at 85 to 90.degree.
C. so as to produce transparent 10% by weight aqueous solution.
[0072] A water content, a dynamic contact angle, wettability, and
an oxygen permeability coefficient of the plastic article, produced
in a manner similar to that in Example 11, except that the
aforementioned methyl vinyl ether-maleic anhydride copolymer was
used instead of the isobutylene-maleic anhydride copolymer in
Example 11, were measured. The results thereof are shown in Table
2.
Comparative Example 5
[0073] A plastic article was produced in a manner similar to that
in Example 11, except that the treatment with the aqueous solution
containing isobutylene-maleic anhydride copolymer in Example 11 was
omitted. A water content, a dynamic contact angle, wettability, and
an oxygen permeability coefficient of the resulting plastic article
are shown in Table 2.
Example 13
[0074] A surface-treated plastic article was produced in a manner
similar to that in Example 9, except that the monomers in Example 9
were changed to 30 parts by weight of
tris(trimethylsiloxy)silylpropyl methacrylate (abbreviated as
TRIS), 30 parts by weight of the compound M2 (abbreviated as
SiMAA2), and 40 parts by weight of 2-hydroxyethyl methacrylate
(abbreviated as HEMA). A water content, a dynamic contact angle,
wettability, a modulus, and an elongation at breakof the resulting
plastic article are shown in Table 2.
Comparative Example 6
[0075] A plastic article was produced in a manner similar to that
in Example 13, except that the treatment with the aqueous solution
containing polyacrylic acid in Example 13 was omitted. A water
content, a dynamic contact angle, and wettability of the resulting
plastic article are shown in Table 2.
Example 14
[0076] 100 parts by weight of 2-hydroxyethyl methacrylate
(abbreviated as HEMA), 1 part by weight of triethylene glycol
dimethacrylate (abbreviated as 3G), and 0.2 parts by weight of
"Darocur1173" manufactured by Ciba Specialty Chemicals were
uniformly mixed, and were photopolymerized using an insect
collection lamp in a manner similar to that in Example 1. The
resulting polymer was released from the molds in purified water,
and thereafter, was subjected to a boiling treatment at 120.degree.
C. for 30 minutes in purified water using an autoclave so as to
produce hydrogel. This hydrogel was immersed in an aqueous solution
containing 5% by weight of polyacrylic acid, having a molecular
weight of 150,000, at 40.degree. C. for 8 hours. Subsequently, the
resulting hydrogel was sufficiently washed with purified water, was
put in a vial containing a boric acid buffer solution having a pH
of 7.1 to 7.3, and was sealed. The resulting vial was put in an
autoclave, and was subjected to a boiling treatment at 120.degree.
C. for 30 minutes. After the vial was left standing for cooling,
the plastic article was taken out of the vial, and was immersed in
the boric acid buffer solution having a pH of 7.1 to 7.3. A water
content, a dynamic contact angle, and wettability of the resulting
plastic article were measured. The results thereof are shown in
Table 2.
Comparative Example 7
[0077] A plastic article was produced in a manner similar to that
in Example 14, except that the treatment with the aqueous solution
containing polyacrylic acid in Example 14 was omitted. A water
content, a dynamic contact angle, and wettability of the resulting
plastic article are shown in Table 2.
Example 15
[0078] 52 parts of 2-hydroxyethyl methacrylate, 53.4 parts of
2,6-diisocyanatocaproic acid-.beta.-isocyanatoethyl ester, and 0.01
parts of di-n-butyltin dilaurate were put into a four neck flask
provided with an agitator, a thermometer, a reflux condenser, and a
nitrogen gas inlet, and were agitated at 50.degree. C. in a
nitrogen atmosphere until the absorption assigned to the hydroxyl
group disappeared from an infrared absorption spectrum. Next, 300
parts of the following compound M4 having an average molecular
weight of 3,000 was added into the aforementioned four neck flask,
and the resulting mixture was agitated at 50.degree. C. in a
nitrogen atmosphere until the absorption assigned to the isocyanato
group disappeared from an infrared absorption spectrum so as to
produce siloxane macromer having two double-bonds at each of both
ends (abbreviated as tetra-functional macromer). 4
[0079] A surface-treated plastic article was produced in a manner
similar to that in Example 8, except that the monomers in Example 8
were changed to 30 parts by weight of the aforementioned
tetra-functional macromer, 38 parts by weight of
tris(trimethylsiloxy)silylpropyl methacrylate (abbreviated as
TRIS), and 32 parts by weight of N,N-dimethylacrylamide
(abbreviated as DMAA). A water content, a dynamic contact angle,
wettability, a modulus, an elongation at break, and an oxygen
permeability coefficient of the resulting plastic article were
measured. The results thereof are shown in Table 3.
Comparative Example 8
[0080] A plastic article was produced in a manner similar to that
in Example 15, except that the treatment with the aqueous solution
containing polyacrylic acid in Example 15 was omitted. A water
content, a dynamic contact angle, wettability, a modulus, an
elongation at break, and an oxygen permeability coefficient of the
resulting plastic article were measured. The results thereof are
shown in Table 3.
Example 16
[0081] 33 parts by weight of the compound M2 (abbreviated as
SiMAA2), 33 parts by weight of the following macromer having
double-bond at one end (abbreviated as single-functional macromer)
M5 with a molecular weight of about 1,000, 5
[0082] 34 parts by weight of N,N-dimethylacrylamide (abbreviated as
DMAA), 5 parts by weight of the following macromer (abbreviated as
double-functional macromer) M6 having a molecular weight of about
1,900, 6
[0083] and 10 parts by weight of ethylene glycol diacetate
(abbreviated as EGDA) were uniformly mixed. After 0.2 parts by
weight of "Darocur1173" manufactured by Ciba Specialty Chemicals,
as a polymerization initiator, was added thereto, a plastic article
to be treated was produced in a manner similar to that in Example
1.
[0084] On the other hand, methyl vinyl ether-maleic anhydride
copolymer having a molecular weight of about 2,000,000 ("Gantrez"
AN-169, manufactured by International Specialty Products Inc.) was
dispersed in purified water, and the resulting solution was
agitated at 85 to 90.degree. C. so as to produce transparent 5% by
weight aqueous solution.
[0085] In this polymer aqueous solution, the aforementioned plastic
article to be treated was immersed at 40.degree. C. for 3 hours.
Subsequently, the resulting plastic article was sufficiently washed
with purified water, was put in a vial containing a boric acid
buffer solution having a pH of 7.1 to 7.3, and was sealed. The
resulting vial was put in an autoclave, and was subjected to a
boiling treatment at 120.degree. C. for 30 minutes. After the vial
was left standing for cooling, the plastic article was taken out of
the vial, and was immersed in the boric acid buffer solution having
a pH of 7.1 to 7.3. A water content, a dynamic contact angle,
wettability, a modulus, and an elongation at break were measured.
The results thereof are shown in Table 3.
Comparative Example 9
[0086] A plastic article was produced in a manner similar to that
in Example 16, except that the treatment with the aqueous solution
containing methyl vinyl ether-maleic anhydride copolymer in Example
16 was omitted. A water content,.a dynamic contact angle,
wettability, a modulus, and an elongation at break of the resulting
plastic article were measured. The results thereof are shown in
Table 3.
Example 17
[0087] The plastic article, treated with polyacrylic acid, produced
according to Example 9 was immersed in an aqueous solution
containing 0.05% of polyacrylicamide, having a molecular weight of
about 1,000,000, at 40.degree. C. for 8 hours. Subsequently, the
resulting plastic article was sufficiently washed with purified
water, was put in a vial containing a boric acid buffer solution
having a pH of 7.1 to 7.3, and was sealed. The resulting vial was
put in an autoclave, and was subjected to a boiling treatment at
120.degree. C. for 30 minutes. After the vial was left standing for
cooling, the plastic article was taken out of the vial, and was
immersed in the boric acid buffer solution having a pH of 7.1 to
7.3. The resulting plastic article had a water content of 32.8%, a
dynamic contact angle of 34.degree., a modulus of 105 psi, and an
elongation at break of 750%. These values indicated that the nature
of the surface was changed compared to that in the case in which
only the treatment with polyacrylic acid was performed so as to
exhibit the water content of 31%, the dynamic contact angle of 280,
the modulus of 91 psi, and the elongation at breakof 561%.
[0088] In order to confirm this point, an adsorption experiment of
lysozyme from egg white was performed. 0.5 g of lysozyme from egg
white was dissolved into 100 ml of boric acid buffer solution so as
to prepare an artificial foul solution. A sheet of sample was
immersed in 1 ml of the resulting foul solution, and was left
standing at 35.degree. C. for 20 hours. After completion of the
immersion treatment, the sample was taken out and was left standing
in the boric acid buffer solution for 5 hours. Thereafter the
resulting sample was pulled up and was lightly wiped to remove
water. An amount of the adsorbed lysozyme was determined by
measuring absorbance at 562 nm using a Micro BCA Protein Assay
Reagent Kit manufactured by Pierce Chemical Co., based on a
bicinconic acid protein assay method. As a consequence, the
adsorption amount in the article treated with polyacrylic acid only
was 33 .mu.g/cm.sup.2, although the adsorption amount in the
article further treated with the immersion in the polyacrylamide
aqueous solution was significantly changed to 150
.mu.g/cm.sup.2.
Example 18
[0089] 99 parts by weight of methyl methacrylate (abbreviated as
MMA), and 1 part by weight of triethylene glycol dimethacrylate
(3G) were uniformly mixed. After 0.1 part by weight of
2,2'-azobis-(2,4-dimethylvaleronitrile- ) (abbreviated as ADVN) as
a polymerization initiator was added thereto, the resulting monomer
mixture was degassed in an argon atmosphere. The degassed monomer
mixture was injected between glass plates and sealed. The
polymerization was performed at 40.degree. C. for 10 hours.
Subsequently, the temperature was raised from 40.degree. C. to
90.degree. C. over a period of time 24 hours, and was kept at
100.degree. C. for 4 hours so as to produce the plastic article to
be treated. The resulting plastic article to be treated was
immersed in an aqueous solution, having a pH of 2.6, containing 5%
by weight of polyacrylic acid having an average molecular weight of
150,000 at 60.degree. C. for 24 hours. Thereafter, the resulting
plastic article was sufficiently washed with purified water. A
water content, a static contact angle of water, and wettability of
the resulting plastic article were measured. The results thereof
are shown in Table 4.
Comparative Example 10
[0090] A plastic article was produced in a manner similar to that
in Example 18, except that the treatment with the aqueous solution
containing polyacrylic acid in Example 18 was omitted. A water
content, a static contact angle of water, and wettability of the
resulting plastic article were measured. The results thereof are
shown in Table 4.
Example 19
[0091] 39 parts by weight of tetra-functional macromer produced
according to Example 15, 49.4 parts by weight of trifluoroethyl
methacrylate (abbreviated as 3FM), 4.1 parts by weight of methyl
methacrylate (abbreviated as MMA), 4.5 parts by weight of
trimethylolpropane trimethacrylate (abbreviated as TMPT), 3 parts
by weight of methacrylic acid (abbreviated as MAA), 0.02 parts by
weight of azobisisobutyronitrile (abbreviated as AIBN), and 0.08
parts by weight of azobiscyclohexanecarbonitrile (abbreviated as
ACHCN) were mixed and dissolved so as to produce a monomer mixture.
The resulting mixture solution was put in a test tube, the monomer
mixture was degassed in an argon atmosphere, and thereafter, the
test tube was plugged airtight. First, in a constant temperature
water bath, heating was performed at 40.degree. C. for 40 hours, at
50.degree. C. for 24 hours, at 60.degree. C. for 16 hours, at
70.degree. C. for 4 hours, and at 90.degree. C. for 2 hours, and
furthermore, in a hot-air circulation type oven, the heating was
performed at 130.degree. C. for 30 hours so as to produce a
rod-like plastic article. The resulting plastic article was cut
into the shape of a circle with a diamond cutter, and the surface
thereof was polished so as to produce a plastic article to be
treated. The plastic article to be treated was immersed in an
aqueous solution, having a pH of 2.6, containing 5% by weight of
polyacrylic acid having an average molecular weight of 25,000 at
60.degree. C. for 8 hours. Subsequently, the resulting plastic
article was sufficiently washed with purified water, was immersed
in a boric acid buffer solution having a pH of 7.1 to 7.3 in a
vial, and the vial was sealed. The resulting vial was put in an
autoclave, and was subjected to a boiling treatment at 120.degree.
C. for 30 minutes. After the vial was left standing for cooling,
the plastic article was taken out of the vial, and was immersed in
the boric acid buffer solution having a pH of 7.1 to 7.3. A water
content, a static contact angle of water, and wettability of the
resulting plastic article were measured. The results thereof are
shown in Table 4.
Comparative Examples 11
[0092] A plastic article was produced in a manner similar to that
in Example 19, except that the treatment with the aqueous solution
containing polyacrylic acid in Example 19 was omitted. A water
content, a static contact angle of water, and wettability of the
resulting plastic article were measured. The results thereof are
shown in Table 4.
[0093] According to the present invention, a surface-treated
plastic article can be provided, in which the surface thereof has
superior hydrophilicity not varying with time while maintaining
various properties as the plastic article.
[0094] In particular, in the case in which the surface-treated
plastic articles are optical articles, for example, contact lenses,
intraocular lenses, and plastic lenses, the aforementioned superior
properties are exhibited, so that superior products can be
produced.
1 TABLE 1 Comp. Comp. Comp. Example Example Example Example Example
Example 1 2 3 1 4 5 2 6 7 8 3 Polymerization composition TRIS 60
21.33 SiOEMMA 68.75 42.67 SiMAA2 70 SiMMA3 70 TRIS-A DMAA 40 20.83
30 36 MEAA 10.42 HEMA 3G 1 Diglyme 10 Darocur 1173 0.2
Macromolecule aqueous solution Macromolecule Polyacrylic acid --
Polyacrylic Polyethylen- -- Polyacrylic acid -- acid eimine
Molecular weight 25,000 5,000 250,000 -- 25,000 600 -- 25,000
150,000 -- Concentration 15 20 1.2 -- 15 wt % 30 wt % -- 15 wt % 5
wt % -- pH 2.3 2.0 3.1 -- 2.3 11.78 -- 2.3 2.3 2.6 -- Immersion
conditions 40.degree. C./8 hr -- 60.degree.C./24 r 23.degree. C./72
hr -- 40.degree. C./8 hr -- Properties of treated article Water
content 29% 30% 26% 27% 30% 27% 25% 27% 18% 34% 30% Dynamic contact
angle 46.degree. 37.degree. 37.degree. 74.degree. 43.degree.
78.degree. 82.degree. 71.degree. 71.degree. 29.degree. 91.degree.
Wettability .circleincircle. .circleincircle. .largecircle.
.circleincircle. Modulus 157 psi 196 psi 171 psi 251 psi 81 psi 73
psi 114 psi 256 psi 74 psi 132 psi Elongation at break 330% 530%
651% 437% 100% 292% 424% 82% 473% 542% Oxygen permeability 95 100
87 92 coefficient* *unit: 10.sup.-11(cm.sup.2/sec)[mlO.sub.2/(ml
.multidot. hPa)]
[0095]
2 TABLE 2 Example Comp. Comp. Comp. Example 9 Example 4 10 11 12
Example 5 Example 13 Example 6 Example 14 Example 7 Polymerization
composition TRIS 31.5 30 30.5 30 SiOEMMA SiMAA2 31.5 30.5 30 SiMMA3
TRIS-A 30 DMAA 37 40 39 MEAA HEMA 40 100 3G 1 Diglyme 10 1 10
Darocur 1172 0.2 Macromolecule aqueous solution Macromolecule
Polyacrylic -- Polyacrylic Isobutylene- Methyl vinyl -- Polyacrylic
-- Polyacrylic -- acid acid Maleic ether-Maleic acid acid anhydride
anhydride copolymer copolymer Molecular 150,000 -- 25,000 160,000
to 216,000 -- 150,000 -- 150,000 -- weight 170,000 Concentration 5
wt % -- 15 wt % 1 wt % 10 wt % -- 5 wt % -- 5 wt % -- pH 2.6 -- 2.3
2.82 2.04 -- 2.6 -- 2.6 -- Immersion 40.degree. C./8 hr --
40.degree. C./8 hr 40.degree. C./5 hr -- 40.degree. C./8 hr --
40.degree. C./8 hr -- conditions Properties of treated article
Water content 31% 29% 38% 38.8% 36.3% 30.6% 13% 11% 42.9% 39%
Dynamic 28.degree. 78.degree. 52.degree. 47.degree. 30.degree.
72.degree. 39.degree. 75.degree. 29.degree. 70.degree. contact
angle Wettability .circleincircle. .circleincircle.
.circleincircle. .circleincircle. .circleincircle. .circleincircle.
Modulus 91 psi 125 psi 79 psi 338 psi Elongation at 561% 359% 159%
61% break Oxygen 90 96 82 85 92 permeability coefficient* *unit:
10.sup.-11(cm.sup.2/sec)[mlO.sub.2/(ml .multidot. hPa)]
[0096]
3 TABLE 3 Comp. Comp. Example 15 Example 8 Example 16 Example 9
Polimerization composition Tetra-functional 30 macromer TRIS 38
SiMAA2 33 Single-functional 33 macromer DMAA 32 34 3G 1 Double 5
functionalmacromer Diglyme 10 EGDA 10 Darocur 1173 0.2
Macromolecule aqueous solution Macromolecule Polyacrylic -- Methyl
vinyl -- acid ether-Maleic anhydride copolymer Molecular weight
150,000 -- 2,000,000 -- Concentration 5 wt % -- 5 wt % -- PH 2.6 --
2.16 -- Immersion 40.degree. C./8 hr -- 40.degree. C./3 hr --
conditions Properties of treated article Water content 22% 20%
33.5% 30.4% Dynamic contact 31.degree. 88.degree. 49.degree.
76.degree. angle wettability .circleincircle. .circleincircle.
Modulus 210 psi 218 psi 95 psi 94 psi Elongation at break 156% 160%
200% 270% Oxygen 118 120 permeability coefficient* *unit:
10.sup.-11(cm.sup.2/sec)[mlO.sub.2/(ml .multidot. hPa)]
[0097]
4 TABLE 4 Comp. Comp. Example Example 8 Example 9 Example 19 11
Polymerization composition MMA 99 4.1 Tetra-functional 39 macromer
3FM 49.44 3G 1 TMPT 4.5 ADVN 0.1 AIBN 0.02 ACHCN 0.08 Macromolecule
aqueous solution Macromolecule Polyacrylic -- Polyacrylic -- acid
acid Molecular weight 150,000 -- 25,000 -- Concentration 5 wt % --
5 wt % -- pH 2.6 -- 2.6 -- Properties of treated articles Immersion
60.degree. C./24 hr -- 60.degree. C./8 hr -- conditions Water
content 0.8% 0.4% 1% 0.5% Static contact angle 35.degree.
73.degree. 83.degree. 100.degree. Wettability .largecircle.
.circleincircle.
* * * * *